ClinVar Miner

List of variants in gene SMARCAL1 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 69
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014140.4(SMARCAL1):c.1851+293T>G rs284551 0.72070
NM_014140.4(SMARCAL1):c.2528+68T>C rs284523 0.36760
NM_014140.4(SMARCAL1):c.2528+131A>G rs205980 0.36752
NM_014140.4(SMARCAL1):c.2071-136T>C rs2129119 0.30191
NM_014140.4(SMARCAL1):c.2529-153T>G rs284524 0.24357
NM_014140.4(SMARCAL1):c.1711-132G>A rs2738284 0.24087
NM_014140.4(SMARCAL1):c.1335-91G>A rs2271334 0.21490
NM_014140.4(SMARCAL1):c.1852-153A>G rs66931264 0.09543
NC_000002.12:g.216483194T>C rs17559422 0.09481
NM_014140.4(SMARCAL1):c.2070T>C (p.Thr690=) rs2066527 0.09474
NM_014140.4(SMARCAL1):c.812-104T>C rs71577872 0.09217
NM_014140.4(SMARCAL1):c.1096+152A>G rs3816784 0.05438
NM_014140.4(SMARCAL1):c.812-156T>C rs2306638 0.05421
NM_014140.4(SMARCAL1):c.2428-95G>A rs58959714 0.05403
NM_014140.4(SMARCAL1):c.2528+198C>T rs78149672 0.05399
NM_014140.4(SMARCAL1):c.945C>G (p.Ser315Arg) rs2066522 0.04294
NM_014140.4(SMARCAL1):c.1129G>C (p.Glu377Gln) rs2066518 0.03294
NM_014140.4(SMARCAL1):c.1645-56T>C rs3816783 0.03291
NM_014140.4(SMARCAL1):c.1335-23A>G rs2066521 0.03286
NM_014140.4(SMARCAL1):c.2626-33C>T rs71579835 0.03207
NM_014140.4(SMARCAL1):c.-58-210G>A rs73072254 0.03100
NM_014140.4(SMARCAL1):c.-58-254G>A rs58617956 0.03050
NM_014140.4(SMARCAL1):c.862+183G>A rs73072255 0.02379
NM_014140.4(SMARCAL1):c.1711-106C>T rs79491615 0.02193
NM_014140.4(SMARCAL1):c.2141+17T>C rs2066516 0.02186
NM_014140.4(SMARCAL1):c.2626-191G>T rs79008053 0.02062
NM_014140.4(SMARCAL1):c.812-89G>A rs75546339 0.02043
NM_014140.4(SMARCAL1):c.811+156T>C rs79736801 0.02034
NM_014140.4(SMARCAL1):c.2428-350G>T rs75259438 0.01750
NM_014140.4(SMARCAL1):c.1711-119C>T rs284549 0.01720
NM_014140.4(SMARCAL1):c.1711-283C>A rs16856180 0.01658
NM_014140.4(SMARCAL1):c.2071-296G>A rs74434188 0.01640
NM_014140.4(SMARCAL1):c.2070+43A>T rs78230573 0.01628
NM_014140.4(SMARCAL1):c.1096+32A>C rs2066515 0.01592
NM_014140.4(SMARCAL1):c.127G>A (p.Ala43Thr) rs2066524 0.01441
NM_014140.4(SMARCAL1):c.423T>C (p.Tyr141=) rs35907255 0.00906
NM_014140.4(SMARCAL1):c.901C>G (p.Pro301Ala) rs146084305 0.00795
NM_014140.4(SMARCAL1):c.1243A>G (p.Ser415Gly) rs58848916 0.00775
NM_014140.4(SMARCAL1):c.341G>A (p.Arg114His) rs11555797 0.00657
NM_014140.4(SMARCAL1):c.1534G>A (p.Val512Met) rs35087810 0.00342
NM_014140.4(SMARCAL1):c.603G>C (p.Gly201=) rs35048226 0.00259
NM_014140.4(SMARCAL1):c.1212G>A (p.Ala404=) rs2066525 0.00241
NM_014140.4(SMARCAL1):c.1995C>T (p.Ala665=) rs151241914 0.00237
NM_014140.4(SMARCAL1):c.1271A>T (p.Asp424Val) rs2066520 0.00215
NM_014140.4(SMARCAL1):c.2528+15G>A rs200879397 0.00078
NM_014140.4(SMARCAL1):c.1850G>T (p.Arg617Leu) rs199805996 0.00068
NM_014140.4(SMARCAL1):c.124A>G (p.Ile42Val) rs199905841 0.00059
NM_014140.4(SMARCAL1):c.962G>A (p.Gly321Asp) rs148752234 0.00047
NM_014140.4(SMARCAL1):c.1785C>T (p.Ile595=) rs145825654 0.00029
NM_014140.4(SMARCAL1):c.270C>T (p.His90=) rs150591090 0.00029
NM_014140.4(SMARCAL1):c.2226G>A (p.Thr742=) rs2271335 0.00009
NM_014140.4(SMARCAL1):c.2649C>T (p.Tyr883=) rs182217350 0.00008
NM_014140.4(SMARCAL1):c.1056C>T (p.Asp352=) rs775747796 0.00003
NM_014140.4(SMARCAL1):c.72A>G (p.Arg24=) rs199805770 0.00001
NM_014140.4(SMARCAL1):c.1645-274C>T rs77349113
NM_014140.4(SMARCAL1):c.1711-111G>T rs284550
NM_014140.4(SMARCAL1):c.1852-205A>C rs2738286
NM_014140.4(SMARCAL1):c.1947C>T (p.Asp649=) rs2066526
NM_014140.4(SMARCAL1):c.2141+56dup rs34170201
NM_014140.4(SMARCAL1):c.2244+19T>C
NM_014140.4(SMARCAL1):c.2625+116dup rs5838586
NM_014140.4(SMARCAL1):c.340C>G (p.Arg114Gly) rs202031614
NM_014140.4(SMARCAL1):c.811+36_811+38del rs5838583
NM_014140.4(SMARCAL1):c.811+37_811+38del rs5838583
NM_014140.4(SMARCAL1):c.811+38del rs5838583
NM_014140.4(SMARCAL1):c.862+128del rs3214962
NM_014140.4(SMARCAL1):c.863-39C>G rs73988775
NM_014140.4(SMARCAL1):c.960C>T (p.Ala320=) rs2066513
NM_014140.4(SMARCAL1):c.961G>A (p.Gly321Ser) rs371378288

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.